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Recruiting NCT07483606

Turkish Validity and Reliability Study of PRevention of Toxic Chemicals in the Environment for Children Tool

Observational Healthy Adult Participants Toxic Chemicals Environmental Toxins

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Healthy Adult Participants, Toxic Chemicals, Environmental Toxins. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Turkish Validity and Reliability Study of PRevention of Toxic Chemicals in the Environment for Children Tool (PRoTECT)

Overview

The aim of this study is to conduct a Turkish validity and reliability study of the "Prevention of Toxic Chemicals in the Environment for Children Tool," developed to examine the knowledge and attitudes of parents and prospective parents regarding the effects of toxic chemicals in the environment on children's development.

Primary outcome measures

  • "Prevention of Toxic Chemicals in the Environment for Children Tool" Turkish validity and reliability [Time frame: 1 months]
  • The Relationship Between Knowledge and Attitudes Towards Prevention of Toxic Chemicals in the Environment for Children and Environmental Literacy [Time frame: 1 months]

Eligibility criteria

Inclusion criteria

Adult parents and prospective parents

Exclusion criteria

Illiterate

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Other

Study locations

Turkey (Türkiye) · 1 center
  • Rukiye Duman — Istanbul

Identifiers

NCT: NCT07483606 · IstanbulUC-EBE-RD-03

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗